Oxidation of hexaaquoiron(II) by periodate in aqueous acidic solution
โ Scribed by Fouad.R. El-Eziri; Yousif Sulfab
- Publisher
- Elsevier Science
- Year
- 1977
- Tongue
- English
- Weight
- 429 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0020-1693
No coin nor oath required. For personal study only.
โฆ Synopsis
The oxidation of Fe(H) by periodate in aqueous acidic solutions obeys the rate law (i)
Rate
= {k, + k,/[fl]} [Fe(H)]' + kk'[Wll)l W-IT WI + k3 [Wll)l 2 [L-l T where [L61T represents the total periodate concentration. The magnitudes of k,,, k;, ky and k3 are 0.235 set-', 120 set-', 7.5 f 1.5 set-I, and (7.3 f 0.5) X 104p set? respectively at 25 'Cand I = 1.0 h4. The ttW?IS in equation (i), that are first order in [L-]T, correspond to the oxidation process with possibly one-electron (term showing first order in [FefII)] and two electron-transfer (term showing second order in [Fe(II)] . At low [fl (0.10 M), the pathway first order in [Fe(IZ)] predominates, whereas at high [H+j (0.80 M), the term second order in [Fe(II)] prevails. An explanation of the term independent of [L-IT is not quite obvious.
๐ SIMILAR VOLUMES
The kinetics of oxidation of CoEDTA2-by periodate follow the rate law (i) Rate = k&l [CoEDTA2-I F-1 1 +Kl[L-] Where [L-l is the total periodate concentration, k3 is the rate constant for the electron-transfer process, and K, is the pre-equilibrium formation constant. Activation parameters are report
Thermal and photochemical oxidations of Fe(bpy)sz+ (bpy=2,2'-bipyridine) by the periodate anion IO,-in acidic aqueous solution were studied. For the thermal process, the rate-limiting step is monomolecular dissociation of the iron(D) complex preceding the fast oxidation by IO,-. Photo-oxidation of F